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Published on: February 5, 2022
Synthesis, Structure, and Magnetic Properties of an Fe36 Dimethylarsinate Cluster: The Largest "Ferric Wheel"
Kenneth Hong Kit Lee1, Lucas Aebersold2, Juan E Peralta2
1Department of Chemistry, University of Florida, Gainesville, Florida32611-7200, United States.
Abstract:
The synthesis and characterization of a high-nuclearity FeIII/O/arsinate cluster is reported within the salt [Fe36O12(OH)6(O2AsMe2)63(O2CH)3(H2O)6](NO3)12 (1). The compound was prepared from the reaction of Fe(NO3)3·9H2O, dimethylarsinic acid (Me2AsO2H), and triethylamine in a 1:2:4 molar ratio in acetonitrile. The Fe36 cation of 1 is an unprecedented structural type consisting of nine Fe4 butterfly units of two types, three {FeIII4(μ3-O)2} units A, and six {FeIII4(μ3-O)(μ3-OH)} units B, linked by multiple bridging Me2AsO2- groups into an Fe36 triangular wheel/loop with C3 crystallographic and D3 virtual symmetry that looks like a guitar plectrum. The unusual structure has been rationalized on the basis of the different curvatures of units A and B, the presence of intra-Fe36 hydrogen bonding, and the tendency of Me2AsO2- groups to favor μ3-bridging modes. The cations stack into supramolecular nanotubes parallel to the crystallographic c axis and contain badly disordered solvent and NO3- anions. The cation of 1 is the highest-nuclearity "ferric wheel" to date and also the highest-nuclearity Fe/O cluster of any structural type with a single contiguous Fe/O core. Variable-temperature direct-current magnetic susceptibility data and alternating-current in-phase magnetic susceptibility data indicate that the cation of 1 possesses an S = 0 ground state and dominant antiferromagnetic interactions. The Fe2 pairwise J couplings were estimated by the combined use of a magnetostructural correlation for high-nuclearity FeIII/oxo clusters and density functional theory calculations using broken-symmetry methods and the Green's function approach. The three methods gave satisfyingly similar J values and allowed the identification of spin-frustration effects and the resulting relative spin-vector alignments and thus rationalization of the S = 0 ground state of the cation.
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